Canonical Allele Identifier: CA884186396

Gene: INSR

Linked Data

• dbSNP Id: rs1172216328
• gnomAD v3: 19-7150256-TC-T
• gnomAD v4: 19-7150256-TC-T
• MyVariant Identifiers: chr19:g.7150268del (hg19) ; chr19:g.7150257del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150259del , CM000681.2:g.7150259del	GRCh38
NC_000019.9:g.7150270del , CM000681.1:g.7150270del	GRCh37
NC_000019.8:g.7101270del	NCBI36
NG_008852.2:g.148744del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2267+240del MANE Select	ENSP00000303830.4:n.2267+240del
ENST00000302850.9:c.2267+240del	ENSP00000303830.4:n.2267+240del
ENST00000341500.9:c.2231+2469del	ENSP00000342838.4:n.2231+2469del
NM_000208.2:c.2267+240del	NP_000199.2:n.2267+240del
NM_000208.3:c.2267+240del	NP_000199.2:n.2267+240del
NM_001079817.1:c.2231+2469del	NP_001073285.1:n.2231+2469del
NM_001079817.2:c.2231+2469del	NP_001073285.1:n.2231+2469del
XM_011527988.1:c.2345+240del	XP_011526290.1:n.2345+240del
XM_011527989.1:c.2309+2469del	XP_011526291.1:n.2309+2469del
XM_011527988.2:c.2267+240del	XP_011526290.2:n.2267+240del
XM_011527989.3:c.2231+2469del	XP_011526291.2:n.2231+2469del
NM_000208.4:c.2267+240del MANE Select	NP_000199.2:n.2267+240del
NM_001079817.3:c.2231+2469del	NP_001073285.1:n.2231+2469del